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PMID: 9764843 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Patients with allergic contact dermatitis to nickel and nonallergic individuals display different nickel-specific T cell responses. Evidence for the presence of effector CD8+ and regulatory CD4+ T cells.

The Journal of investigative dermatology ·Vol. 111 ·No. 4 ·1998-10-00 ·Pages 621-8

Cavani A, Mei D, Guerra E, Corinti S, Giani M, Pirrotta L, Puddu P, Girolomoni G

Abstract

To investigate the mechanisms underlying the expression of allergic contact dermatitis, we compared the characteristics of nickel (Ni)-specific T cell responses in 10 patients with allergic contact dermatitis to Ni and in 10 healthy, nonallergic individuals. CD4+ T cells purified from peripheral blood of both allergic and nonallergic subjects proliferated similarly to NiSO4 in vitro, with the responses mostly restricted to CD4+ CD45RO+ memory T cells. In contrast, Ni-specific CD8+ T cell responses were detected only in allergic patients. Limiting dilution assay confirmed a high frequency of Ni-specific CD4+ T cells in both individual categories, and of Ni-specific CD8+ T cells in allergic patients, but not in nonallergic persons. Ni-specific CD4+ T cell clones prepared from nonallergic subjects displayed lower interferon-gamma and higher interleukin-10 production compared with T cell clones from allergic patients. The T cell skin-homing receptor, cutaneous lymphocyte-associated antigen, was expressed on the large majority of specific CD4+ clones from both the groups. Finally, Ni-specific CD8+ clones prepared from patients also expressed the cutaneous lymphocyte-associated antigen receptor, and released high interferon-gamma and no interleukin-4. In aggregate, the results suggest that the presence of specific CD8+ T cells and a distinct pattern of cytokine release (e.g., an augmented production of interleukin-10) by CD4+ T cells can be important elements in determining whether a hapten induces allergy or a silent immune response.

MeSH Terms
Adult Antigens, Differentiation, T-Lymphocyte Antigens, Neoplasm CD4-Positive T-Lymphocytes/cytology,immunology CD8-Positive T-Lymphocytes/cytology,immunology Cell Division/drug effects Dermatitis, Allergic Contact/etiology,immunology,pathology Dermatitis, Contact/etiology,immunology,pathology Female Humans Immunologic Memory Interferon-gamma/metabolism Interleukin-10/metabolism Irritants/pharmacology Male Membrane Glycoproteins/analysis Nickel/adverse effects,pharmacology Phenotype T-Lymphocyte Subsets/metabolism
Chemicals
Antigens, Differentiation, T-Lymphocyte Antigens, Neoplasm CTAGE1 protein, human Irritants Membrane Glycoproteins Interleukin-10 nickel sulfate Nickel Interferon-gamma
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Cavani A
Laboratory of Immunology, Istituto Dermopatico dell'Immacolata, IRCCS, Rome, Italy.
Mei D
Guerra E
Corinti S
Giani M
Pirrotta L
Puddu P
Girolomoni G
Article Info
Journal
The Journal of investigative dermatology
Abbr.
J Invest Dermatol
ISSN
0022-202X
Published
1998-10-00
Pages
621-8
Language
English
Region
United States
NLM ID
0426720
Subset
IM
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